1114-00-7 Usage
Description
()-2,3-dibromosuccinic acid is a chemical compound with the molecular formula C4H4Br2O4. It is a crystalline solid that is used in organic synthesis and as a reagent in biochemical research. ()-2,3-dibromosuccinic acid is a derivative of succinic acid, with two bromine atoms attached to the 2 and 3 positions on the succinic acid molecule. Its structure and properties make it useful in the study of stereochemistry and chiral molecules.
Uses
Used in Organic Synthesis:
()-2,3-dibromosuccinic acid is used as a reactant in organic reactions for the synthesis of various compounds. Its unique structure with bromine atoms allows for specific reactivity and functional group transformations, making it a valuable intermediate in the preparation of complex organic molecules.
Used in Biochemical Research:
As a reagent in biochemical research, ()-2,3-dibromosuccinic acid is utilized for studying stereochemistry and chiral molecules. Its distinct properties enable researchers to investigate the behavior of chiral compounds and their interactions with biological systems, contributing to a deeper understanding of molecular biology and enzymology.
Used in Pharmaceutical Development:
()-2,3-dibromosuccinic acid may have potential applications in the pharmaceutical industry. Its unique structure could be harnessed for the development of new drugs with specific properties, targeting various therapeutic areas. ()-2,3-dibromosuccinic acid's reactivity and functional group compatibility make it a promising candidate for medicinal chemistry research and drug design.
Used as a Building Block for New Compounds:
In addition to its direct applications, ()-2,3-dibromosuccinic acid can serve as a building block for the development of new compounds with specific properties. Its versatility in organic synthesis and compatibility with various functional groups make it an attractive starting material for creating novel molecules with potential applications in various industries, including materials science, agrochemicals, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 1114-00-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1114-00:
(6*1)+(5*1)+(4*1)+(3*4)+(2*0)+(1*0)=27
27 % 10 = 7
So 1114-00-7 is a valid CAS Registry Number.
1114-00-7Relevant articles and documents
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Halpern,J.,Maher,J.P.
, p. 5361 - 5366 (1965)
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Hughes,Watson
, p. 1733,1739 (1930)
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Preparation method of butynedioic acid
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Paragraph 0050-0051, (2020/07/21)
The invention discloses a preparation method of butynedioic acid. The method comprises the following steps of: (1) firstly, carrying out water-free and oxygen-free treatment on a closed reaction kettle; (2) putting calcium carbide, a solvent, a catalyst and an auxiliary agent into the reaction kettle, introducing carbon dioxide into the reaction kettle, and heating and pressurizing for reaction; (3) separating the reacted mixture obtained in the step (2) to obtain a liquid mixture, and adding a KOH solution into the liquid mixture; stirring to separate out a white precipitate; and dissolving the white precipitate in hot water, acidifying with concentrated sulfuric acid, cooling, separating out the white precipitate, and filtering to obtain the product. The synthesis method disclosed by theinvention is relatively environment-friendly and low in production cost.
Kinetic study of the Ce(III)-, Mn(II)-, or ferroin-catalyzed Belousov-Zhabotinsky reaction with pyruvic acid
Lin, Hsing-Lien,Yu, Yueh-O,Jwo, Jing-Jer
, p. 408 - 418 (2007/10/03)
Ce(III)-, Mn(II)-, or ferroin (Fe(phen)32+)-catalyzed reaction of bromate ion and pyruvic acid (PA) or its dimer exhibits oscillatory behavior. Both the open-chain dimer (parapyruvic acid, γ-methyl-γ-hydroxyl-α-keto-glutaric acid, DP
